Hominoid Phylogeny, the C/P3 complex and

Maxillary Canine Microwear in Dryopithecus From Spain

Pierre-Francois PUECH and Bernard PUECH http://independent.academia.edu/pfpuech

Taxonomy and Evolutionary Relationships. Famous figures -as Lamarck or Darwin- have suggested a common ancestor to closely related species, as are the African great apes and humans. The Hominoid (apes and humans), forming a super Family bearing humanlike anatomical characteristics -e.g. having no tail, a relatively high and short skull and the 32 teeth of all the Old World simians with the lower first molar equipped with five cusps whose arrangement is shared with humans. The hominoid lineage became manifest in 1856 with the species Dryopithecus from tertiary territories. But, to-day, it is still difficult to ascertain if this great ape (~ 15 8 Ma old) belongs to pongids or to hominids.

The five-cusp and fissure pattern of the first lower molar teeth of Dryopithecus, known as the Y-5 arrangement, is typical of hominoids in general P.-F. PUECH. The simians have welded the mandible symphysis and mandible occlusion turned to be locked by the engagement of the canines. The projection of the upper canine (lacerative) requires a space (diastema) to fit in the opposite tooth row. Occlusion of upper canine with first lower premolar (C / P3) serves as a sharpener. We retain three functional domains to the C/P3 complex: mesioocclusal wear with the lower canine, tip wear, and distolingual wear facet with a third premolar (Puech P.-F. et al.1989 Maxillary canine microwear in Dryopithecus from Spain. Am. J. Phys. Anthropol.80:305-312). The oldest recovery of an Ape type locomotion has been found by S. Moy Sol, not in Africa but in Catalonia in a 9.5 Myears old Dryopithecus. In Dryopithecus the canine tip are blunt by puncture-crushing , with dentine more worn than enamel in the typical appearance of wear resulting from abrasion, as in gorilla, orang-utan, chimpanzee canines and in early hominids from Laetoli and Hadar (Puech and Albertini, 1984 Dental microwear and mechanisms in early hominid s from Laetoli and Hadar. Am. J. Phys. Anthropol. 65:87-91). Wolpff M.H. reported in PaleoAnthropology (2006: 36-50) that to 1

varying extents, a number of Miocene ape canines evince a canine tip with a similar pattern. The C/P3 complex of our closest ancestors tells a series of events concerning human origins: changes in canine crown shape and reduction of the longest dimension within the hominine clade have eliminated the honing upper canine / lower premolar P3 occlusal specialization of apes. Decrease of the maxillary canine projection has given more occlusal leeway and transformed the dental occlusion function of hominines. Premolars P3 tend to become more molarised providing evidence for the changing biological role of this tooth. The result is that mandibular premolar heteromorphy (P3 compared to P4) is minimal in later hominines, including Homo sapiens.

The morphological evidence used to define humans is reinforced after the divergence from the apes that was carried out 8-7 million years ago. Australopithecines, which have an antiquity of ~ 5 Ma, were bipeds and that is the reason why Homo and Australopithecus are grouped as hominines. But the African apes knuckle-walk may have evolved from some kind of bipedal locomotion shared by the hominines ancestors (Verhaegen M. and Puech P.-F. 2000 Hominid lifestyle and diet reconsidered and comparative data.Hum.Evol. 15: 151-162).

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